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1. Mr. K. Jeganmohan et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 3, Issue 6, Nov-Dec 2013, 1637-1641
RESEARCH ARTICLE
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OPEN ACCESS
A Narrative Experimental View for Zeolite in Molecular
Orientation
Mr. K. Jeganmohan, Dr. K. Jagadeesan, Dr. Aravind Yadav
Research Scholar, Allahabad University
Professor & Head, Civil Dept, Mahendra Engg College
Professor / Environmental dept, Allahabad University
ABSTRACT
In this paper, FTIR spectroscopy in understanding with polarized light and an ATR look into coated with a boriented ZSM-5 film was the first time used to conclude the point of reference of adsorbed molecules in the
ZSM-5 structure. Two adsorbents were studied, n-hexane and p-xylene and the results decided with formerly
reported results obtained by other investigational techniques.
Keywords: Zeolite; Attenuated Total Reflection; adsorbates; dichroic ratio ; gas sensing; silanol ; guest/host
materials; absorption.
I.
INTRODUCTION
Zeolites are widely used in industry as ion
exchangers, sorbents and catalysts and several novel
applications such as membranes for separations and
chemical sensors have been planned. A thorough facts
of the adsorption is basic in all these applications. In
the present work, two systems that have been widely
studied previously, viz. n-hexane/MFI and pxylene/MFI were selected for inquiry by a novel
technique. An overview of the previously reported
results for these systems is given below. Several
groups have studied the n-hexane/MFI system, and an
inflection in the adsorption isotherm has been reported
at a concentration of ca. 0.7 mmol/g, corresponding to
about half the saturation loading [1,2]. The inflection
was credited to adsorption on dissimilar sites by Smit
and Maesen [3], who studied the system using Monte
Carlo simulations.
They observed a redeployment of n-hexane as
the concentration in the adsorbent increased. At low
concentrations, the molecules are evenly spread in the
intersections and in the channels. At higher
concentrations, the molecules migrate into the
sinusoidal channels exit the intersections free, enabling
a complete filling of the straight channels. Mentzen [4]
employed powder x-ray diffraction (XRD) and
observed a similar redistribution of n-hexane at room
temperature. On the contrary, Morell et al. [5] could
not observe any redistribution of the adsorbate at room
temperature nor any favored sites when investigating
the nhexane/silicalite-1 system with powder and single
crystal XRD as well as 29Si MAS NMR and molecular
modelling. However, clear ordering of n-hexane
appeared when the temperature was lowered to 180 K,
with molecules only adsorbed in the channels leaving
the intersections unoccupied.
A type IV isotherm has been observed for pxylene when adsorbed in MFI powder and unsupported
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films at temperatures around- and slightly above room
temperature [6,7]. For the case of a type IV isotherm,
the saturation capacity is 8 molecules/unit cell (or ~1.4
mmol/g). When the temperature is increased, a type I
isotherm with a saturation capacity of only 4 molecules
per unit cell is observed. The location and orientation
of p-xylene molecules in MFI have been studied by
means of XRD [8,9], FTIR microscopy, [10] Monte
Carlo simulations [11] and NMR [12]. The initial step
in the type IV isotherm has been assigned to adsorption
of p-xylene in the intersections with the long axis
(going through the CH3- groups) mainly oriented in
the b-direction of the crystals. Further, the second step
in the type IV isotherm has been assigned to p-xylene
adsorbed in the sinusoidal channels [9]. FTIR/ATR
(Attenuated Total Reflection) has emerged as a
powerful tool for studying surfaces and thin films of
various systems, e.g. polymers [13], mineral flotation
[14], membrane peptides [15], and catalysts [16]. An
advantage with the technique is that, by applying
polarized radiation, it is possible to gain information
on orientation of adsorbed molecules [13-15]. This
work aims at illustrating the utility of FTIR/ATR
spectroscopy combined with polarized radiation and
oriented MFI films for determining the arrangement of
molecules in MFI crystals for the first time. In this
context, an advantage with p-xylene as adsorbate is
that the molecule is rigid, in that it cannot take on
different conformers. This makes it possible to
determine an average tilt angle of the molecule relative
the surface normal.
II.
EXPERIMENTAL METHOD
Trapezoidal (50x20x2 mm, 45° cut edges)
ZnS Attenuated Total Reflection (ATR) elements were
coated with b-oriented ZSM-5 films using an in-situ
method [17]. The films were subsequently
characterized by Scanning Electron Microscopy (SEM)
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2. Mr. K. Jeganmohan et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 3, Issue 6, Nov-Dec 2013, 1637-1641
and XRD [17]. The infrared measurements were
conducted using a Bruker IFS 66v/S spectrometer
prepared with a liquid nitrogen cooled mercury
cadmium telluride (MCT) detector. Polarized radiation
was achieved by applying a rotatable ZnSe wire grid
polarizer. A gas delivery system and an insitucell were
used for exposing the film to a controlled environment,
details of the equipment have been reported previously
[18]. Helium (AGA 99.99990%) was used as carrier
gas and n-hexane (Sigma 99+%) and p-xylene (Aldrich
99+%) were used as adsorbates. Prior to each
measurement, the film was heated in-situ to 573 K for
4 hours at a heating/cooling rate of 1°/min. under a
flow of pure helium to remove any molecules adsorbed
in the zeolite. Subsequently, the cell was mounted in
the spectrometer and background spectra without
polarizer, and with 0° and 90° division were recorded
by averaging 128 scans. After that the hydrocarbon
was introduced and spectra were recorded at
equilibrium by averaging 64 scans. First one spectrum
was recorded without polarizer, and then spectra with
0°, 90° and 0° polarization were recorded. Two spectra
were recorded at 0° to ensure that the system was
stable. In the evaluation, the mean value of the two
measurements at 0° was used. IR spectra recorded
without polarizer were used for determining the
concentration of the adsorbate in the film, whereas
spectra recorded with polarized radiation were used for
determining the dichroic ratio. For n-hexane, the peak
height of the methylene asymmetric stretching
vibration band (2934 /cm) was used for determining
the dichroic ratio, whereas for p-xylene, the integrated
absorbance of a band assigned to a ring stretching
vibration (1518 /cm) was used for formative the
dichroic ratio.
2.1 The ATR-technique
In the ATR sampling technique, the infrared
radiation is reflected inside a waveguide, also denoted
an ATR element. At each reflection, a standing wave
of the electromagnetic field is created. This field
penetrates a short detachment outside the element
surface and interacts with molecules situated close to
the element surface. The concentration of the
electromagnetic field decays exponentially with
distance from the surface and a penetration depth, dp,
has been
introduced to estimate the surface sensitivity of the
technique [19]:
The wavelength of the radiation in the
element is λ1, θ is the angle of incidence (45° in this
work), and n21= n2/n1 is the ratio of the refractive
indices in the film (n2), and element (n1), respectively.
The penetration depth is usually in the range from a
couple of hundred nm to a few µm, making the ATR
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technique especially well suited for studying thin
films.
As pointed out in the foreword, an benefit
with the ATR-technique is that it is possible to
conclude average molecular orientation by applying
polarized radiation. The key parameter when
determining the direction of molecules is the dichroic
ratio, D, and by assuming an uniaxial distribution of
the adsorbates, the dichroic ratio is given by [20]:
The absorbance for a certain band resolute
with radiation polarized in the plane of the element
surface is denoted As (s-polarized) and Ap is the
absorbance for the same band recorded with radiation
polarized in the plane normal to the element surface,
see Figure 1. Moreover, Ө is the angle between the
transition moment of the vibration of interest and the
main axis of the molecule, for p-xylene, Ө = 0° for the
ring stretching vibration observed at
1518 /cm. Further, γ is the tilt angle of the main
molecule axis from the surface normal.
The electric field amplitudes, Ex, Ey and Ez,
in the x-,y- and z-directions are given for a three layer
system (ATR-element, film and gas) by equations, 3, 4
and 5.
The refractive index of the gas is denoted n3
and n31=n3/n1 and n32=n3/n2. By inserting Ө = 0° in
equation.2 a simplified version of the equation is
obtained:
From this expression, γ can be determined
after measuring the dichroic ratio and calculating Ex,
Ey and Ez from equation 3 to equation 5.
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3. Mr. K. Jeganmohan et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 3, Issue 6, Nov-Dec 2013, 1637-1641
III.
RESULTS AND DISCUSSION
Figures 2 (a) and (b) show top- and side view
images of a ZSM-5 film on a ZnS element. The images
indicate that the film mostly consists of inter grown boriented crystals with tablet habit, and a slight fraction
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of a-oriented crystals. Further, a few b-oriented
crystals are deposited on top of the film. The images
also show that the film did not cover the element
entirely.
The adsorption of n-hexane in a silicalite-1
film developed from seeds and found that the
saturation capacity was in superior agreement with
standards reported for powders. By assuming that the
result reported by Bjorklund et al. is valid also for the
films used in this study, a parameter accounting for
discrepancies both due to deficient surface coverage
and to any differences in molar absorptivity between
the experimental value determined in CCl4 and the real
value in the zeolite can be defined. The parameter,
khexane, was determined to about 0.43. Spectra recorded
without polarizer of n-hexane and p-xylene adsorbed in
the film were very similar to previously reported
spectra,
examples
are
shown
in
Fig.3.
As expected, for n-hexane, bands appear in
the CH stretching region between 3000-2700 /cm and
in the CH deformation vibration region between 15001300 /cm. In the
p-xylene spectrum, several
overlapping bands appear in the region 3200-2700 /cm,
from which the most prominent are the bands at 2924
and 2869 /cm, assigned as symmetric methyl stretching
vibration and asymmetric methyl deformation overtone
[10]. At lower wave numbers, bands appear at 1518,
1456 and 1376 /cm, these bands are assigned to
benzene ring stretching vibration, asymmetric and
symmetric
methyl
deformation
vibrations,
respectively. In addition, for both spectra, a negative
band appears at 3730 /cm in combination with the
appearance of a new band at lower wave numbers.
This band is assigned to silanol groups perturbed by
adsorbate molecules resulting in a shift to lower wave
numbers.
Spectra recorded with the polarized radiation
showed significant polarization of several bands and
examples are shown in Fig. 4.
The bands indicated in the spectra were the
ones used for determining the dichroic ratio, and in all
cases, higher absorbance was observed with ppolarized radiation. The strong polarization, mostly
observed in spectra of p-xylene, indicate a preferential
orientation of the molecules. Dichroic ratios
determined at different concentrations are presented in
Table 1 together with calculated tilt angles for p-
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4. Mr. K. Jeganmohan et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 3, Issue 6, Nov-Dec 2013, 1637-1641
xylene. The dichroic ratio for n-hexane changes
significantly when the concentration changes from
0.60 to 0.85 mmol/g, i.e. in the region where the
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inflection have been reported, while the ratio changes
less in the concentration range 0.85 – 1.42 mmol/g.
Table 1. Dichroic ratio at different adsorbate concentrations in the film.
The change in dichroic ratio in the
concentration range 0.66 – 0.84 mmol/g indicates that
some kind of molecular reorientation takes place. A
change in the conformer distribution, i.e. the number of
trans C-C bonds, could cause a change in the dichroic
ratio for alkanes. However, the positions of the CH2stretching vibrations bands are known to be sensitive
to the conformation of alkanes. Shifts to lower wave
numbers indicate that the number of trans bonds
increases whereas a shift to higher wave numbers is a
sign of an increased number of gauche bonds. In the
present study, the position of the asymmetric CH2stretching vibration band was fairly constant at 2934
/cm throughout the concentration range studied.
Hence, the change in the dichroic ratio
observed in the present work at about half the
saturation loading is attributed to a redistribution of nhexane in concert with the findings of Smit and
Maesen [3] and Mentzen [4]. Further, if all n-hexane
molecules were in all-trans conformation it would have
been possible to determine an average molecular
orientation, however previous studies have shown that
this is not the case for n-hexane in MFI, hence no
average tilt angles for n-hexane were determined in the
present work.
For p-xylene, we observe a decrease in
dichroic ratio and average tilt angle with increasing
concentration. The tilt angle 20° obtained at a
concentration of 0.73 mmol/g is very close to the one
reported by Schüth (18°), as determined by FTIR
microscopy on large single crystals at ca 310 K [10].
van Koningsveld et al. [9] investigated the pxylene/MFI system at room temperature using XRD
and found a tilt angle of 7.5° for p-xylene adsorbed in
the channel intersections. Fyfe et al. [12] employed
1
H/29Si CP MAS NMR spectroscopy to study the
pxylene/ ZSM-5 system and found that the orientation
of p-xylene in the intersection that best fitted
experimental data is with the long axis parallel to the
crystallographic b-direction.However, the authors
states that completely reliable data was only obtained
below 213 K and data recorded above room
temperature could not be used for distance and
structure determinations due to extensive molecular
motions averaging the interactions. The difference in
tilt angle between the measurements in this report and
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the ones by van Koningsveld et al and Fyfe et al. may,
at least partially, be explained by molecules being
more mobile at the higher temperatures used in the
present study. Further, some involvement may also
create from p-xylene adsorbed on silanol groups, as
indicated in Figure 3. Aggressive adsorption on silanol
groups may also explain the observed decrease in tilt
angle with increasing concentration in the present
work.
In addition to being a tool for studying
molecular orientation, the FTIR/ATR technique has
high sensitivity, making it appropriate for studying the
properties of very thin films. Moreover, since FTIR
spectroscopy is sensitive to the species adsorbed, it
should be possible to determine the orientation of
adsorbed molecules from a multi component mixture
as long as the direction of the transition moments are
known and the corresponding absorption bands are
separated. Another interesting application would be to
use the technique to study anisotropic diffusion in
zeolites. A challenge for quantitative measurements is
the need of a molar extinction coefficient for the
adsorbate in the zeolite film. Furthermore, the small
size of the crystals constituting the film introduces
some problems. Firstly, the large external surface
area/volume ratio leads to relatively high concentration
of external silanol groups, which may affect the
quantitative measurements as well as the determination
of adsorbate orientation. A second effect is that small
crystals in a dense film results in more grain
boundaries and some of these will always be open,
enabling capillary compression to occur may also
influence the data.
IV.
CONCLUSIONS
A novel technique for studying the orientation
of adsorbates in zeolite at various concentrations of the
adsorbate was developed. The method utilizes ATR
elements coated with oriented zeolite films in mixture
with FTIR spectroscopy and was demonstrated by
studying the adsorption of n-hexane and p-xylene in a
b-oriented ZSM-5 film. The obtained results agreed
with previous findings.
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5. Mr. K. Jeganmohan et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 3, Issue 6, Nov-Dec 2013, 1637-1641
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